Motor Neurone Disease, fighting it together.

Hello, my name is Lesley Roberts and my husband Christopher, who was a farmer, was diagnosed with MND on May 5th 2014, sadly he lost his courageous fight with this awful disease on September 5th 2015. I wrote this blog to ,share our journey as a family with this disease, the good days and the the bad days and hope to raise awareness of MND in the process. (Follow on Google+ or on Twitter for updates at @soulpunkpixie, or sign up at the bottom of the page for email notification.)

Saturday, 28 June 2014

No.11.Time to smile

Today is our youngest daughter`s 19th birthday. It isn`t time to dwell on regrets for the future, but to celebrate today and bloody well have some fun. You ain`t taking this away from us MND.!
Posted by soulpixie at 06:52
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Blog Archive

  • ▼  2014 (141)
    • ▼  June (14)
      • No.1.Confirmation = devastation
      • No.2.Facing reality
      • No.3.Life goes on.
      • No.4.Trying to stay positive.
      • No.5.Privacy and normality.
      • No.6.The voice expresses our soul .
      • No.7.Being normal
      • No.8.Kindness in it`s many ways
      • No.9.Manifestations of festiculations
      • No.10.Time to adjust, time to think
      • No.11.Time to smile
      • No.12.Memories made.
      • No.13.Stolen futures.
      • No.14.Virtual hugs.
    • ►  July (30)
    • ►  August (31)
    • ►  September (23)
    • ►  October (24)
    • ►  November (10)
    • ►  December (9)
  • ►  2015 (129)
    • ►  January (11)
    • ►  February (12)
    • ►  March (8)
    • ►  April (8)
    • ►  May (17)
    • ►  June (13)
    • ►  July (19)
    • ►  August (23)
    • ►  September (8)
    • ►  October (3)
    • ►  November (2)
    • ►  December (5)
  • ►  2016 (12)
    • ►  January (5)
    • ►  February (5)
    • ►  March (2)

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